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The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates
Vacuolar-type H(+) ATPases (V-ATPases) are multimeric protein complexes that play a universal role in the acidification of intracellular compartments in eukaryotic cells. We have isolated the recessive medaka mutation tintachina (tch), which carries an inactivating modification of the conserved glyc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827601/ https://www.ncbi.nlm.nih.gov/pubmed/24225653 http://dx.doi.org/10.1038/srep03217 |
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author | Müller, Claudia Maeso, Ignacio Wittbrodt, Joachim Martínez-Morales, Juan R. |
author_facet | Müller, Claudia Maeso, Ignacio Wittbrodt, Joachim Martínez-Morales, Juan R. |
author_sort | Müller, Claudia |
collection | PubMed |
description | Vacuolar-type H(+) ATPases (V-ATPases) are multimeric protein complexes that play a universal role in the acidification of intracellular compartments in eukaryotic cells. We have isolated the recessive medaka mutation tintachina (tch), which carries an inactivating modification of the conserved glycine residue (G75R) of the proton pump subunit atp6v1Ba/vatB1. Mutant embryos show penetrant pigmentation defects, massive brain apoptosis and lethality before hatching. Strikingly, an equivalent mutation in atp6v1B1 (G78R) has been reported in a family of patients suffering from distal renal tubular acidosis (dRTA), a hereditary disease that causes metabolic acidosis due to impaired kidney function. This poses the question as to how molecularly identical mutations result in markedly different phenotypes in two vertebrate species. Our work offers an explanation for this phenomenon. We propose that, after successive rounds of whole-genome duplication, the emergence of paralogous copies allowed the divergence of the atp6v1B cis-regulatory control in different vertebrate groups. |
format | Online Article Text |
id | pubmed-3827601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38276012013-11-15 The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates Müller, Claudia Maeso, Ignacio Wittbrodt, Joachim Martínez-Morales, Juan R. Sci Rep Article Vacuolar-type H(+) ATPases (V-ATPases) are multimeric protein complexes that play a universal role in the acidification of intracellular compartments in eukaryotic cells. We have isolated the recessive medaka mutation tintachina (tch), which carries an inactivating modification of the conserved glycine residue (G75R) of the proton pump subunit atp6v1Ba/vatB1. Mutant embryos show penetrant pigmentation defects, massive brain apoptosis and lethality before hatching. Strikingly, an equivalent mutation in atp6v1B1 (G78R) has been reported in a family of patients suffering from distal renal tubular acidosis (dRTA), a hereditary disease that causes metabolic acidosis due to impaired kidney function. This poses the question as to how molecularly identical mutations result in markedly different phenotypes in two vertebrate species. Our work offers an explanation for this phenomenon. We propose that, after successive rounds of whole-genome duplication, the emergence of paralogous copies allowed the divergence of the atp6v1B cis-regulatory control in different vertebrate groups. Nature Publishing Group 2013-11-14 /pmc/articles/PMC3827601/ /pubmed/24225653 http://dx.doi.org/10.1038/srep03217 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Müller, Claudia Maeso, Ignacio Wittbrodt, Joachim Martínez-Morales, Juan R. The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates |
title | The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates |
title_full | The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates |
title_fullStr | The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates |
title_full_unstemmed | The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates |
title_short | The medaka mutation tintachina sheds light on the evolution of V-ATPase B subunits in vertebrates |
title_sort | medaka mutation tintachina sheds light on the evolution of v-atpase b subunits in vertebrates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827601/ https://www.ncbi.nlm.nih.gov/pubmed/24225653 http://dx.doi.org/10.1038/srep03217 |
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